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5-Isoquinolinesulfonic acid, 4-[(2S)-2-[[(1,1-dimethylethoxy)carbonyl]methylamino]-3-[4-(4-iodophen yl)-1-piperazinyl]-3-oxopropyl]phenyl ester

Base Information Edit
  • Chemical Name:5-Isoquinolinesulfonic acid, 4-[(2S)-2-[[(1,1-dimethylethoxy)carbonyl]methylamino]-3-[4-(4-iodophen yl)-1-piperazinyl]-3-oxopropyl]phenyl ester
  • CAS No.:516473-15-7
  • Molecular Formula:C34H37IN4O6S
  • Molecular Weight:756.661
  • Hs Code.:
  • Mol file:516473-15-7.mol
5-Isoquinolinesulfonic acid,
4-[(2S)-2-[[(1,1-dimethylethoxy)carbonyl]methylamino]-3-[4-(4-iodophen
yl)-1-piperazinyl]-3-oxopropyl]phenyl ester

Synonyms:

Suppliers and Price of 5-Isoquinolinesulfonic acid, 4-[(2S)-2-[[(1,1-dimethylethoxy)carbonyl]methylamino]-3-[4-(4-iodophen yl)-1-piperazinyl]-3-oxopropyl]phenyl ester
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 5-Isoquinolinesulfonic acid, 4-[(2S)-2-[[(1,1-dimethylethoxy)carbonyl]methylamino]-3-[4-(4-iodophen yl)-1-piperazinyl]-3-oxopropyl]phenyl ester Edit
Chemical Property:
Purity/Quality:
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Technology Process of 5-Isoquinolinesulfonic acid, 4-[(2S)-2-[[(1,1-dimethylethoxy)carbonyl]methylamino]-3-[4-(4-iodophen yl)-1-piperazinyl]-3-oxopropyl]phenyl ester

There total 3 articles about 5-Isoquinolinesulfonic acid, 4-[(2S)-2-[[(1,1-dimethylethoxy)carbonyl]methylamino]-3-[4-(4-iodophen yl)-1-piperazinyl]-3-oxopropyl]phenyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
1-[(S)-N-tert-butyloxycarbonyl-N-methyltyrosyl]-4-(4-iodophenyl)piperazine; With sodium hydride; In tetrahydrofuran; for 0.166667h;
5-isoquinolinesulfonyl chloride; In tetrahydrofuran; dichloromethane; at 20 ℃; for 18h;
DOI:10.1021/jm021049d
Guidance literature:
Multi-step reaction with 2 steps
1.1: 92 percent / EDC; HOBt / dimethylformamide / 24 h / 20 °C
2.1: NaH / tetrahydrofuran / 0.17 h
2.2: 98 percent / tetrahydrofuran; CH2Cl2 / 18 h / 20 °C
With sodium hydride; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jm021049d
Guidance literature:
Multi-step reaction with 2 steps
1.1: 92 percent / EDC; HOBt / dimethylformamide / 24 h / 20 °C
2.1: NaH / tetrahydrofuran / 0.17 h
2.2: 98 percent / tetrahydrofuran; CH2Cl2 / 18 h / 20 °C
With sodium hydride; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jm021049d
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